chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
82297528022975281TA40GENICpossibly homozygous52537094
82297568522975686TC29GENIChomozygous52537096
82297617422976175AG32GENIChomozygous52537098
82297619722976198TC33GENIChomozygous52537100
82297714122977142TC50GENIChomozygous52537102
82297733222977333TA34GENIChomozygous52537104
82297814022978141GA27GENIChomozygous52537116
82297886022978861TC26GENIChomozygous52537122
82297983622979837TC29GENIChomozygous52537129
82297852022978521TTG7GENICpossibly homozygous53602054
82297852822978529TTGTGTGTGTGTGTG4GENIChomozygous53602058
82297982922979833AAAT----9GENIChomozygous53602060
82297985222979853TC20GENIChomozygous53602062
82298057222980573GGTGTGTGTGTGTGTATGTGTC4GENICheterozygous53602064
82298062022980621GGTGTGTC7GENIChomozygous53602069
82298185822981859CT34GENIChomozygous52537141
82298242722982428TG35GENIChomozygous52537143
82298292022982921TC15GENICpossibly homozygous52537149
82297924022979241T-21GENICheterozygous53569691
82298249922982500TG43GENIChomozygous52537145
82298272122982722TC34GENIChomozygous52537147
82298293222982933AAC16GENIChomozygous52537151
82298300222983003AAG10GENIChomozygous52537153